Autori: Maver Ales
Naslov | Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (Article) |
Autori | Ruml-Stojanovic Jelena Miletic Aleksandra Peterlin Borut Maver Ales Mijovic Marija Borlja Nikola Dimitrijevic Brankica Soldatovic Ivan A ![]() |
Info | JOURNAL OF CHILD NEUROLOGY, (2020), vol. 35 br. 2, str. 116-131 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Clinical Next Generation Sequencing Reveals An H3f3a Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth Retardation (Article) |
Autori | Maver Ales Cuturilo Goran Stojanovic Ruml J Peterlin Borut |
Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 65-68 |
Projekat | Slovenian Research Agency - Slovenia [J3-8205, J3-9280, P3-0326] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Rare missense TUBGCP5 gene variant in a patient with primary microcephaly (Article) |
Autori | Maver Ales Cuturilo Goran Kovanda Anja Miletic Aleksandra Peterlin Borut |
Info | EUROPEAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 62 br. 12, str. - |
Projekat | ARRS research programme [P3-0326, J3-8205, J3-5506] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice (Article) |
Autori | Tumiene B Maver Ales Writzl Karin Hodzic A Cuturilo Goran Kuzmanic-Samija Radenka Culic V Peterlin Borut |
Info | CLINICAL GENETICS, (2018), vol. 93 br. 5, str. 1057-1062 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases (Article) |
Autori | Bergant Gaber Maver Ales Lovrecic Luca Cuturilo Goran Hodzic Alenka Peterlin Borut |
Info | GENETICS IN MEDICINE, (2018), vol. 20 br. 3, str. 303-312 |
Projekat | Slovenian Research Agency [P3-0326] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis (Article) |
Autori | Maver Ales ... Drulovic Jelena S ![]() ![]() ![]() |
Info | SCIENTIFIC REPORTS, (2017), vol. 7 br. , str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility (Article) |
Autori | Hodzic Alenka Ristanovic Momcilo Zorn Branko Tulic Cane Dz Maver Ales Novakovic Ivana V ![]() |
Info | ANDROLOGY, (2017), vol. 5 br. 1, str. 70-74 |
Projekat | Slovenian Research Agency [P3-0326] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility (Article) |
Autori | Hodzic Alenka Ristanovic Momcilo Zorn Branko Tulic Cane Dz Maver Ales Novakovic Ivana V ![]() |
Info | PLOS ONE, (2013), vol. 8 br. 3, str. - |
Projekat | National Research Agency of the Republic of Slovenia [P3-0326] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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